Epix Therapeutics

FDA Filings

This page includes the latest FDA filings for Epix Therapeutics. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3015180993
FEI Number3015180993
NameEPIX THERAPEUTICS
Owner & OperatorEpix Therapeutics
Contact Address8200 Coral Sea Street NE MVS46
Mounds View MN 55112 US
Official Correspondent
  • Jennifer Anderson
  • x-763-5262566-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address945 Stewart Drive Suite 100
Sunnyvale, CA 94085 US
Establishment TypeManufacture Device in the United States for Export Only



FDA Filings

Device
Company
DeviceDate
EPIX THERAPEUTICS
Powercord2019-03-26
EPIX THERAPEUTICS
Footswitch, DiamondTemp? RFG2019-03-26
EPIX THERAPEUTICS
FASTR Generator2019-03-26
EPIX THERAPEUTICS
DiamondTempTM RF Generator2019-03-26
EPIX THERAPEUTICS
DiamondTemp?Irrigation Tubing Set2019-03-26
EPIX THERAPEUTICS
DiamondTemp? Unidirectional Ablation Catheter (small curve)2019-03-26
EPIX THERAPEUTICS
DiamondTemp? Unidirectional Ablation Catheter (large curve)2019-03-26
EPIX THERAPEUTICS
DiamondTemp? Irrigation Pump2019-03-26
EPIX THERAPEUTICS
DiamondTemp? GenConnect Cable2019-03-26
EPIX THERAPEUTICS
DiamondTemp? Catheter-to-RFG Cable2019-03-26
EPIX THERAPEUTICS
DiamondTemp? Bidirectional Ablation Catheter (small curve)2019-03-26
EPIX THERAPEUTICS
DiamondTemp? Bidirectional Ablation Catheter (large curve)2019-03-26
EPIX THERAPEUTICS
DiamondTemp Ablation System2019-03-26

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